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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364095Generated: October 30, 2026

Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → HCID 66743438, compound

https://huagongshe.com/reaction/2364095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantSodium BicarbonateHCID 516892—
Reactant3-amino-5-(5-methyl-1H-pyrazol-4-yl)thiophene-2-carboxamideHCID 66743013—
SolventDimethylacetamideHCID 31374—
ProductHCID 66743438HCID 6674343825.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-amino-5-(5-methyl-1H-pyrazol-4-yl)thiophene -2-carboxamide (100 mg, 0.45 mmol), 1-benzylpiperidin-4-one (0.093 mL, 0.50 mmol), CSA (125 mg, 0.54 mmol), MgSO4 (108 mg, 0.90 mmol) and DMA (1 mL) was stirred at 100° C. for 3 h. The mixture was poured into saturated aqueous NaHCO3. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, and then dried over Na2SO4. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (Purif, NH, 90:10 hexane/EtOAc to EtOAc then to 90:10 EtOAc/MeOH), then crystallized from MeOH/EtOAc/hexane to give the title compound (45 mg, 25%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-2799cc9e3b6945539b5c5ffd1c53d60d
Source noteuspto-grants-2014_04